Rajbhog Sweets Yellow Jalebi Net Weight: 10 oz. UPC 3542647018 packaged in a plastic container and in bulk sold by weig
Summary
The FDA issued a Class II for Rajbhog Sweets Yellow Jalebi Net Weight: 10 oz. UPC 3542647018 packaged in a pl by Rajbhog Distributors, Inc. Reason: Product label lists "butter" on the but does not include the common name for the allergen "milk".
Details
Source
Food Recall
External ID
F-0761-2023
Action Date
2023-05-03
Status
Terminated
Category
food
Product Description
Rajbhog Sweets Yellow Jalebi Net Weight: 10 oz. UPC 3542647018 packaged in a plastic container and in bulk sold by weight
Lot/Code Info: Best by date: 04/05/23
Quantity Affected: 469 units and 305 pounds
Reason for Recall
Product label lists "butter" on the but does not include the common name for the allergen "milk"
Distribution
Dallas, Plano, Frisco, Irving, Sugarland and Austin Texas areas.
Type: Voluntary: Firm initiated
Recall Initiated: 2023-02-10
Company
Dallas, TX
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 28 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Rajbhog Distributors, Inc has 2 FDA actions in our database, including 2 recalls.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Rajbhog Distributors, Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Rajbhog Distributors, Inc have FDA actions?
Rajbhog Distributors, Inc has 2 FDA actions in our database, including 2 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0761-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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